Epitaxial phase diagrams of SrTiO3, CaTiO3, and SrHfO3: Computational investigation including the role of antiferrodistortive and A-site displacement modes

Article

关键词: INITIO MOLECULAR-DYNAMICS;    TOTAL-ENERGY CALCULATIONS;    AUGMENTED-WAVE METHOD;    THIN-FILMS;    BASIS-SET;    CRYSTAL;    STRAIN;    FERROELECTRICITY;    POLARIZATION;    TRANSITION;   

DOI  :  10.1103/PhysRevB.97.134103

来源: SCIE

【 摘 要 】

Ground-state epitaxial phase diagrams are calculated by density functional theory (DFT) for SrTiO3, CaTiO3, and SrHfO3 perovskite-based compounds, accounting for the effects of antiferrodistortive and A-site displacement modes. Biaxial strain states corresponding to epitaxial growth of (001)-oriented films are considered, with misfit strains ranging between-4% and 4%. Ground-state structures are determined using a computational procedure in which input structures for DFT optimizations are identified as local minima in expansions of the total energy with respect to strain and soft-mode degrees of freedom. Comparison to results of previous DFT studies demonstrates the effectiveness of the computational approach in predicting ground-state phases. The calculated results show that antiferrodistortive octahedral rotations and associated A-site displacement modes act to suppress polarization and reduce the epitaxial strain energy. A projection of calculated atomic displacements in the ground-state epitaxial structures onto soft-mode eigenvectors shows that three ferroelectric and six antiferrodistortive displacement modes are dominant at allmisfit strains considered, with the relative contributions from each varying systematically with the strain. Additional A-site displacement modes contribute to the atomic displacements in CaTiO3 and SrHfO3 , which serve to optimize the coordination of the undersized A-site cation.

【 授权许可】

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